6 results
algorithm hyponatremia metabolic table alkalosis chloride defects epithelial hypokalemia hypotonic kidney management nagma nonaniongap normal pathophysiology physiologic syndrome uricacid urinary
Inherited Defects in Kidney Tubule Epithelial Cells Renal glucosuria - Na+-dependent glucose cotransporter Cystinuria - Amino acid transporter Bartter
Inherited Defects ... ascending limb Gitelman ... acidosis - alpha-Intercalated ... Defects #Kidney #Nephrology ... #Diagnosis #Differential
Hyponatremia Differential Diagnosis Algorithm - Utilizing Uric Acid ADH promotes Urea/uric acid excretion along with water
Hyponatremia Differential ... Diagnosis Algorithm ... salt wasting By Rachel ... #nephrology #sodium ... #low #uricacid
Gitelman Syndrome Overview What? • Inherited (AR) hypokalemic salt-losing tubulopathies affecting the thiazide-sensitive sodium chloride cotransporter • Gitelman's syndrome
• Inherited (AR) ... alkalosis • Normal or low ... acidosis (RTA)) ... #Syndrome #diagnosis ... #nephrology #management
Metabolic Alkalosis - Urinary Chloride Algorithm Cl- responsive metabolic alkalosis • Kidney loss of Cl-
alkalosis • Normal/low ... Bartter syndrome, Gitelman ... urine #Algorithm #nephrology ... #differential # ... diagnosis
Normal Anion-Gap Acidosis (NAGMA) - Differential Diagnosis Framework and Workup NAGMA - Chem, ABG or VBG - Calculate Anion
(NAGMA) - Differential ... Diagnosis Framework ... Losses via NGT tube ... #Diagnosis #Workup ... #nephrology
Physiologic Approach to Hypotonic Hyponatremia The next time you have a case of hypotonic hyponatremia, give the
algorithm Urine Na+K / serum ... can be high or low ... #Hyponatremia #differential ... #diagnosis #table ... #sodium #nephrology
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